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Acta Paediatrica; Jul1998, Vol. 87 Issue 7, p811-813, 3p, 1 Chart, 1 Graph
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Koppelhus, Uffe; Tranebjaerg, L; Esberg, G; Ramsing, M; Lodahl, M; Rendtorff, N D; Olesen, H V; Sommerlund, Mette; Esberg, Gitte; Lodahl, Marianne; Rendtorff, Nanna Dahl
Koppelhus , U , Tranebjaerg , L , Esberg , G , Ramsing , M , Lodahl , M , Rendtorff , N D , Olesen , H V , Sommerlund , M , Koppelhus , U , Tranebjaerg , L , Esberg , G , Ramsing , M , Lodahl , M , Rendtorff , N D , Olesen , H V & Sommerlund , M 2011 , ' A novel mutation in the connexin 26 gene (GJB2) in a child with clinical and histological features of keratitis-ichthyosis-deafness (KID) syndrome ' , Clinical and Experimental Dermatology , vol. 36 , no. 2 , pp. 142-8 .
Electronic Resource
Fluge , G , Olesen , H V , Gilljam , M , Meyer , P , Pressler , T , Storrösten , O T , Karpati , F & Hjelte , L 2009 , ' Co-morbidity of cystic fibrosis and celiac disease in Scandinavian cystic fibrosis patients ' , Journal of Cystic Fibrosis , vol. 8 , no. 3 , pp. 198-202 .
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[AR] Olesen, H V
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